Cyanide intermediates in catalytic reduction of NO by C2H4 on Rhodium(III)

Temp.-programmed reaction spectroscopy and secondary ion mass spectrometry (SIMS) have been applied to study reactions of NO and C2H4 coadsorbed on Rh(111). As expected, H2O, CO2, and N2 are the main products at low C2H4 coverages, but at higher coverages H2, HCN, CO, and NO, and even some C2N2 evolve as well. Static SIMS indicates the formation of a large supply of adsorbed cyanide species, part of which desorbs as HCN, while the remainder decomps. and is responsible for delayed formation of N2. For the highest C2H4 coverages, the majority of the nitrogen atoms in the initially adsorbed NO desorbs as HC

Surface reactions of nitrogen oxide and ethylene on rhodium(111)

Where H2, H20, CO2 and N2 are the main products at low C2H4 coverages, ignificant amounts of HCN, CO and NO evolve at higher C2H4 coverages. Static SIMS indicates the formation of a large supply of adsorbed CN species, part of which desorbs as HCN, while the remainder decomposes and is responsible for delayed formation of N2. For the highest C2H4 coverages the majority of the initi-ally adsorbed NO desorbs as HCN

Cyanide intermediates in catalytic reduction of NO by C2H4 on Rhodium(III)

Temp.-programmed reaction spectroscopy and secondary ion mass spectrometry (SIMS) have been applied to study reactions of NO and C2H4 coadsorbed on Rh(111). As expected, H2O, CO2, and N2 are the main products at low C2H4 coverages, but at higher coverages H2, HCN, CO, and NO, and even some C2N2 evolve as well. Static SIMS indicates the formation of a large supply of adsorbed cyanide species, part of which desorbs as HCN, while the remainder decomps. and is responsible for delayed formation of N2. For the highest C2H4 coverages, the majority of the nitrogen atoms in the initially adsorbed NO desorbs as HC